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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112685copy number variation1nstd102humannot provided GRCh37 chr1: 2,420,003-8,155,935 , GRCh38.p12 chr1: 2,488,564-8,095,875 LINC02780, C1orf174, 100 more genes
    nsv5682404mobile element insertion1nstd211human GRCh38 chr1: 7,983,790-7,983,790 , GRCh37.p13 chr1: 8,043,850-8,043,850 PARK7
    nsv5673413copy number variation1nstd102humanPathogenic GRCh37 chr1: 7,995,073-8,031,023 , GRCh38.p12 chr1: 7,935,013-7,970,963 PARK7, TNFRSF9
    nsv5401996mobile element insertion1nstd206human GRCh38 chr1: 7,983,790-7,983,833 , GRCh37.p13 chr1: 8,043,850-8,043,893 PARK7
    nsv5072586mobile element insertion1nstd203human GRCh38 chr1: 7,976,466-7,976,480 , GRCh37.p13 chr1: 8,036,526-8,036,540 PARK7
    nsv5060139mobile element insertion1nstd203human GRCh38 chr1: 7,983,774-7,983,790 , GRCh37.p13 chr1: 8,043,834-8,043,850 PARK7
    nsv5033032inversion1nstd200human GRCh38 chr1: 7,616,493-8,198,892 , GRCh37.p13 chr1: 7,676,553-8,258,952 TNFRSF9, CAMTA1, 10 more genes
    nsv4903021copy number variation1nstd200human GRCh38 chr1: 7,960,551-8,000,209 , GRCh37.p13 chr1: 8,020,611-8,060,269 PARK7
    nsv4903020copy number variation1nstd200human GRCh38 chr1: 7,960,415-7,988,545 , GRCh37.p13 chr1: 8,020,475-8,048,605 PARK7
    nsv4903019copy number variation1nstd200human GRCh38 chr1: 7,958,335-7,977,057 , GRCh37.p13 chr1: 8,018,395-8,037,117 PARK7
    nsv4903016copy number variation1nstd200human GRCh38 chr1: 7,909,530-7,968,326 , GRCh37.p13 chr1: 7,969,590-8,028,386 UTS2, PARK7, 2 more genes
    nsv4889673copy number variation1nstd200human GRCh38 chr1: 7,974,093-7,974,220 , GRCh37.p13 chr1: 8,034,153-8,034,280 PARK7
    nsv4889672copy number variation1nstd200human GRCh38 chr1: 7,972,913-7,972,967 , GRCh37.p13 chr1: 8,032,973-8,033,027 PARK7
    nsv4889671copy number variation1nstd200human GRCh38 chr1: 7,968,746-7,969,777 , GRCh37.p13 chr1: 8,028,806-8,029,837 PARK7
    nsv4879676inversion1nstd200human GRCh37 chr1: 7,676,553-8,258,952 , GRCh38.p12 chr1: 7,616,493-8,198,892 TNFRSF9, PARK7, 10 more genes
    nsv4782799copy number variation1nstd200human GRCh37 chr1: 8,034,153-8,034,280 , GRCh38.p12 chr1: 7,974,093-7,974,220 PARK7
    nsv4772133copy number variation1nstd200human GRCh37 chr1: 8,020,611-8,060,269 , GRCh38.p12 chr1: 7,960,551-8,000,209 PARK7
    nsv4772132copy number variation1nstd200human GRCh37 chr1: 8,020,475-8,048,605 , GRCh38.p12 chr1: 7,960,415-7,988,545 PARK7
    nsv4581697copy number variation1nstd183human GRCh37 chr1: 8,015,436-8,304,607 , GRCh38.p12 chr1: 7,955,376-8,244,547 PARK7, ERRFI1, 6 more genes
    nsv4535378insertion1nstd166human GRCh37.p13 chr1: 8,043,834-8,043,834 , GRCh38.p12 chr1: 7,983,774-7,983,774 PARK7
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